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Volumn 284, Issue 5417, 1999, Pages 1187-1191

Inactivation of misselected CD8 T cells by CD8 gene methylation and cell death

Author keywords

[No Author keywords available]

Indexed keywords

FAS ANTIGEN; FAS LIGAND; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; T LYMPHOCYTE RECEPTOR;

EID: 0033553620     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.284.5417.1187     Document Type: Article
Times cited : (77)

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    • PCR primers were selected to span exons and to yield similarly sized single-band products. Sense and antisense primers, respectively, were as follows: β-actin, GACTACCTCATGAAGATCCT and CTAGAAGCACTT- GCGGTGCAC (570 bp); CD8α, GCCAGAAGGTGGAC- CTGGTATGTG and GAGTGATGATCAAGGACAGCA- GAAG (498 bp); CD8β, ATGCAGCCATGGCTCTG- GCTGG and GCATGTCAGGCCCTTCTGGGTC (512 bp); and TCR Cβ, CCCACTATTTTTCTTCCTTCTGTT- GCTGAA and TTTGTTGTTCTCATGTTTGACAATAC- A-ACT (255 bp). CD4 transcripts (615 bp) (Clontech) were always undetectable (9) [X. F. Yang, G. F. Weber, H. Cantor, Immunity 7, 629 (1997)].
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    • We thank H.-S. Teh for the antibody to TCR H-Y, T3.70; P. Marrack for KJ1-26.1 hybridoma (anti- DO11.10 TCR); A. Sharpe for DO11.10 TCR transgenic mice; I. Rimm for the lpr/lpr mutant mice expressing the DO11.10 TCR transgene; G. Stella and X.-f. Yang for advice with the semiquantitative RT- PCR; and A. Angel and K. MacKay for assistance in the preparation of this manuscript. All work involving animals was conducted under protocols approved by the Animal Care and Use Committee at Dana Farber Cancer Institute. Supported by NIH basic research grants CA76176 to G.F.W. and Al 13600 and Al 37833 to H.C.


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